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- Beierle, Elizabeth A1
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Online Exclusives
10 Results
- Rapid Communication
Retroperitoneal lipoblastoma: A discussion of current management
Journal of Pediatric SurgeryVol. 47Issue 10e51–e54Published in issue: October, 2012- Daniela Burchhardt
- Sara C. Fallon
- Monica E. Lopez
- Eugene S. Kim
- John Hicks
- Mary L. Brandt
Cited in Scopus: 12Retroperitoneal lipoblastomas are rare tumors found in young pediatric patients. Despite their large size at presentation, complete resection is usually achieved with minimal complications. Diagnosis is typically made after pathologic examination of the operative specimen, and cytogenetic analysis may be a key component in differentiating lipoblastoma from other lipomatous tumors. We present one such case of a large, retroperitoneal lipoblastoma and discuss the management of this uncommon entity. - Rapid Communication
Benign intrascrotal lipoblastoma in a 4-month-old infant: a case report and review of literature
Journal of Pediatric SurgeryVol. 46Issue 7e9–e12Published in issue: July, 2011- Naglaa Mohamed Kamal
- Riadh Jouini
- Samira Yahya
- Moutaz Haiba
Cited in Scopus: 12Lipoblastomas are rare benign soft tissue tumors that occur primarily in young children. Most lipoblastomas occur in the extremities, trunk, head, and neck. An intrascrotal location is unusual. We describe a case of a 4-month-old infant with an intrascrotal lipoblastoma and discuss the differential diagnosis and review the literature. - Rapid Communication
Lipoblastoma: a rare lesion in the differential diagnosis of childhood mediastinal tumors
Journal of Pediatric SurgeryVol. 46Issue 5e21–e23Published in issue: May, 2011- Randa Salem
- Mohamed Zohd
- Leila Njim
- Kais Maazoun
- Mohamed Ali Jellali
- Ahmed Zrig
- and others
Cited in Scopus: 11Lipoblastoma is a rare, benign, fatty tissue tumor that occurs in childhood. The location of this tumor in the mediastinum and extension to the chest wall is uncommon. We describe a 12-month-old male infant with a mediastinal lipoblastoma discovered because of a chest wall swelling. Computed tomography showed the deep component and fatty content of the lesion suggestive of the diagnosis. Total excision of the mass was carried out. The histologic examination of the lesion confirmed the diagnosis of lipoblastoma. - Rapid Communication
Lipoblastoma with unique localization requiring tracheal and esophageal resection
Journal of Pediatric SurgeryVol. 45Issue 10e21–e23Published in issue: October, 2010- Michele Torre
- Cecilia Borel
- Francisco Saitua
- Francisco Ossandon
- Juan Jose Latorre
- Patricio Varela
Cited in Scopus: 7Lipoblastoma and lipoblastomatosis are rare tumors of infancy. They originate from embryonic fat and localize in soft tissues. We present the case of a lipoblastoma of the neck with localization in tracheal and esophageal walls that required an extended laryngotracheal and esophageal resection. To our knowledge, this is the first report of such localization of this tumor. - Rapid Communication
A tale of 3 testes? A rare presentation of lipoblastoma with a novel karyotype
Journal of Pediatric SurgeryVol. 45Issue 1e29–e31Published in issue: January, 2010- Andrew Robb
- Timothy Rogers
- Guy Nicholls
Cited in Scopus: 7Lipoblastoma is a rare benign mesenchymal tumor of embryonal fat that occurs almost exclusively in infants and children. Although lipoblastomas can affect any part of the body, only 5 cases affecting the scrotum have previously been reported. We present a case of an intrascrotal lipoblastoma with a novel karyotype. - Rapid Communication
Mesenteric lipoblastoma presenting as a segmental volvulus
Journal of Pediatric SurgeryVol. 44Issue 2e25–e28Published in issue: February, 2009- David C. Yu
- Patrick J. Javid
- Kudakwashe R. Chikwava
- Harry P. Kozakewich
- Maria Debiec-Rychter
- Craig W. Lillehei
- and others
Cited in Scopus: 9Mesenteric lipoblastoma is a rare tumor and, its presentation as a bowel obstruction with possible midgut volvulus has only been reported once before. A 7-year-old girl presented with nausea and vomiting but a benign abdominal examination. Upper gastrointestinal contrast study demonstrated possible malrotation with midgut volvulus. During emergency laparotomy, segmental small bowel volvulus secondary to a large mesenteric lipoblastoma was found. The lipoblastoma was resected with a segment of small bowel. - Rapid Communication
Mesenteric lipoblastoma: a rare location in children
Journal of Pediatric SurgeryVol. 43Issue 12e5–e7Published in issue: December, 2008- Raymond Cudnik
- Philip A. Efron
- Mike K. Chen
- John D. Reith
- Elizabeth A. Beierle
Cited in Scopus: 13Lipoblastoma is a rare childhood tumor composed of embryonic fat. It is benign and most often presents in children younger than 3 years. These tumors primarily present as a rapidly enlarging mass in the extremities or trunk with abdominal lipoblastomas comprising less than 10% of all reported cases. Abdominal lipoblastomas are most commonly found in the retroperitoneum with less than 15 reported cases arising in the mesentery. We report the unusual presentation of a lipoblastoma arising in the mesentery of a 3-year-old boy. - Rapid Communication
Lipoblastoma arising from the submandibular region
Journal of Pediatric SurgeryVol. 43Issue 11e13–e15Published in issue: November, 2008- Nam-Yong Do
- Sung-Il Cho
- Jun Hee Park
- Ji Yun Choi
Cited in Scopus: 7A lipoblastoma is a rare, benign tumor arising from embryonic white fat. The tumors occur primarily in infancy and early childhood and commonly arise from the limbs and the trunk, but neck involvement is extremely rare. Our case arose in a 22-month-old male presenting with a rapidly enlarging soft mass in the right submandibular area. Lipoblastoma was diagnosed by histologic evaluation, the mass was completely removed, and there was no recurrence at 1-year follow-up. - Rapid Communication
Intrascrotal lipoblastoma: a case report and review of the literature
Journal of Pediatric SurgeryVol. 42Issue 3e9–e11Published in issue: March, 2007- Rachele Del Sordo
- Antonio Cavaliere
- Angelo Sidoni
- Renato Colella
- Guido Bellezza
Cited in Scopus: 14Lipoblastomas are rare benign soft tissue tumors that occur primarily in young children. Most lipoblastomas occur in the extremities, trunk, head, and neck. An intrascrotal location is unusual. We describe the case of a 4-year-old boy with an intrascrotal lipoblastoma and discuss the differential diagnosis in reviewing the literature. - Rapid Communication
Lipoblastoma of kidney in a child
Journal of Pediatric SurgeryVol. 41Issue 7e29–e30Published in issue: July, 2006- Jirí Morávek
- Jirí Šnajdauf
- Roman Kodet
- Zdenek Hříbal
Cited in Scopus: 4This report describes a very rare case of lipoblastoma of a kidney affecting a small child. A 2-year-old boy was admitted for a palpable mass in the right abdominal quadrant. A preoperative examination revealed a tumor of uncertain origin. A simple nephrectomy was performed. Postoperative histologic examination confirmed lipoblastoma of the kidney. No other therapy was necessary. The child is well, without any sign of the disease 9 years after the tumor removal.